Cleftopedia is here to educate new and existing parents, and in no way is it meant to sway anyone in any direction. Remember – you, the parent, are your child’s best advocate, and only you know what is best for your child.
All the information that is in this website is based on personal experience and is not endorsed by any organization, hospital or surgeons. Chances are you found Cleftopedia because your baby has recently been diagnosed with a cleft lip and/or cleft palate and we want you to know…you are not alone.
In website they present a list of Cleft Teams within the United States (for every state!). In it you will find details about pre-surgical techniques, post-surgical restrictions, age requirements for surgeries, future surgeries required, and so much more. We captured real-life comments about the overall team and surgeon experience, and many mommies have even shared before and after photos of their beautiful babies for you to see actual results.
Accessible Location: No
|Type of Organization||online|
|Categories||Advocacy, Disability Specific, Emotional Support, Other|
|Services offered in Spanish?||No|
|Child Care Available?||No|
|Age Range||All Ages|
|Disability Categories||Physical Disability|
|Does this organization belong to all disabilities?||No|
|This organization belongs to these diagnoses||Cleft Lip and Palate|
|Is this a statewide service?||yes|
|Contact Name||Dara Smith (co-founder)|
|Email Address||[email protected]|